The Recall Desk

State

Massachusetts product recalls

72,907 recalls have nationwide distribution and so reach Massachusetts. 8,208 additional recalls listed Massachusetts specifically in their distribution scope.

What the numbers show

Total
8,208
Critical
1,171
Severe
2,012
Most recent
2026-09-09

Of the 8,208 recalls naming Massachusetts we have scored against our rubric, 1,171 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,012 (25%) are Severe.

These figures cover only the 8,208 recalls whose distribution notice names Massachusetts specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1301–1325 of 81115

  • ModerateFDA (Devices)·Z-2419-2026·2026-06-24

    Medline central line dressing and port kits contain recalled Mastisol

    Medline central line dressing kits, PICC/CVC/midline CHG dressing kits, port-a-cath kits and vein ablation packs are being recalled over a recalled lot of Mastisol Liquid Adhesive.

    Product
    Medline convenience kits: INPATIENT CENTRAL LN DRSG KIT DYNDC3525 PICC/CVC/MIDLINE DRSG CHG KIT DT13191A PORT A CATH CDS982047S VEIN ABLATION PACK DYNJ62889C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2435-2026·2026-06-24

    Medline basic eye and tubal ligation kits contain recalled Mastisol

    The Medline Basic Eye kit and Tubal Ligation CDS kit are being recalled because they contain a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive.

    Product
    Medline convenience kits: BASIC EYE DYNJ905154I TUBAL LIGATION CDS CDS760053K
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0639-2026·2026-06-24

    Med Pride hydrocortisone cream 16oz tubes recalled over manufacturing deviations

    Med Pride Hydrocortisone Cream 1%, 16 oz tubes, is being recalled because of CGMP deviations observed during an FDA inspection. 4,738 tubes are affected.

    Product
    Med Pride, HYDROCORTISONE CREAM 1%, Net Wt. 16oz (454g) tubes, Manufactured for: Shield Line LLC, 59 Hook Road, Bayonne, NJ 07002 USA, Made in India, UPC 3 52410 305061.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0641-2026·2026-06-24

    Med Pride triple antibiotic ointment packets recalled over manufacturing deviations

    Med Pride Triple Antibiotic Ointment in 0.9 g packets is being recalled because of CGMP deviations and deficiencies observed during an FDA inspection. 3,006 tubes affected.

    Product
    Med Pride, Triple Antibiotic Ointment, Bacitracin Zinc (equivalent to 400 units), Neomycin Sulfate 5 mg, Polymixin B 5000 units, 0.9g packets, 144 packets per box, 130g, Manufactured for: Shield Line LLC, 59 Hook Road, Bayonne, NJ 07002 USA, Made in India, UPC 1 03 52410 30253 1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2425-2026·2026-06-24

    Medline IV start kits with HubGuard contain recalled Mastisol adhesive

    The Medline IV Start Kit with HubGuard is being recalled because it contains a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive whose butyrate tubing may crack.

    Product
    Medline convenience kit: IV START KIT W/HUBGUARD DYNDV2662
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2441-2026·2026-06-24

    Medline arthroscopy and paediatric kits contain recalled Mastisol adhesive

    Medline convenience kits for ACL, arthroscopy, back and paediatric procedures are being recalled because they contain a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive.

    Product
    Medline convenience kits: ACL PACK DYNJ64161C ARTHROSCOPY PACK DYNJ47103D DYNJ67197G DYNJ85197A DYNJT4007 BASIC ACCESS PACK-LF DYNJ36698B BASIC BACK TRAY DYNJ89037 BASIC PEDI PACK-LF DYNJ0171446I DYNJ0171446J BASIC SPINE DYNJ910915A BREAST PACK DYN
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2423-2026·2026-06-24

    Medline plastic surgery kits contain recalled Mastisol liquid adhesive

    Medline convenience kits for breast imaging, plastics and facial procedures are being recalled because they contain a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive.

    Product
    Medline convenience kits: BREAST IMAGING DYNJT5893 CHOG PLASTICS SYNJ10306A ENDO BREAST AUGMENTATION PACK DYNJ68023 FACIAL PLASTIC DYNJ909926C JVL - MODULE PLASTIC PK DYNJ84081B KIT MAJOR PLASTICS MOSES DYNJ905362C MEM MAXILLOFACIAL PACK-LF DYNJ0660040
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0591-2026·2026-06-24

    Kerr Insta-Char activated charcoal suspension did not meet OTC monograph

    VistaPharm Kerr Insta-Char activated charcoal in a sorbitol base with cherry flavor is being recalled because the product did not meet the Over-the-Counter Monograph M023.

    Product
    VistaPharm, KERR INSTA-CHAR IN AN SORBITOL BASE WITH CHERRY FLAVOR, 25 Grams Activated Charcoal in 26 Grams Sorbitol in 120 mL (4 fl oz), distributed by: VistaPharm, Inc., Largo. FL 33771, NDC 66689-203-04.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2424-2026·2026-06-24

    Medline basic and laparoscopy packs contain recalled Mastisol liquid adhesive

    Medline convenience kits including basic packs, general laparoscopy, CVC insertion bundles and da Vinci packs are being recalled over a recalled lot of Mastisol Liquid Adhesive.

    Product
    Medline convenience kits: BASIC DYNJ905869G BASIC PACK DYNJ68484B BIB GENERAL LAPAROSCOPY PA DYNJ58305 CHRISTUS CH PEDIATRIC BASIC DYNJ61167G CVC INSERTION BUNDLE CVI3940A DAVINCI PACK SURGICOUNT DYNJ45544F EPCH BASIC PACK DYNJ83094C GENERAL PACK D
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0608-2026·2026-06-24

    Focalin XR 5mg capsules carry incorrect or missing lot and expiry

    Focalin XR 5 mg extended-release capsules are being recalled over a labeling issue: incorrect or missing lot number and/or expiry date. 7,803 bottles are affected.

    Product
    FOCALIN — FOCALIN (DEXMETHYLPHENIDATE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V399000·2026-06-23

    GM Recalls 2025-2026 Savana and Express for Steering Nut Issue

    General Motors is recalling 2025-2026 GMC Savana and Chevrolet Express vehicles because a steering gear nut may be loose, risking loss of control.

    Product
    GMC — GMC, CHEVROLET SAVANA, EXPRESS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26E037000·2026-06-23

    Rockford Fosgate Amplifier Kits Recalled for Fire Risk

    Rockford Corporation is recalling specific amplifier kits because a fuse may fail to protect against short circuits, increasing the risk of a fire.

    Product
    ELECTRICAL SYSTEM:WIRING:FUSES AND CIRCUIT BREAKERS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V400000·2026-06-23

    Hyundai Tucson instrument panel displays may fail due to software error

    Hyundai is recalling certain 2025-2026 Tucson, Tucson Hybrid and Tucson Plug-In Hybrid vehicles because a software error may cause the instrument panel display to fail.

    Product
    HYUNDAI — HYUNDAI TUCSON PLUG-IN HYBRID, TUCSON HYBRID, TUCSON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26E038000·2026-06-23

    Ricon Recalls S-Series and K-Series Wheelchair Platform Lifts

    Ricon is recalling S-Series and K-Series wheelchair platform lifts because a failed electrical contactor may prevent the controls from stopping the lift.

    Product
    EQUIPMENT ADAPTIVE/MOBILITY:WHEELCHAIR LIFT/RAMP:CONTROLS/CONTROL WIRING recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E036000·2026-06-19

    Airxcel Recalls MaxxAir N-Series Maxxfan Fans Due to Overheating Risk

    Airxcel is recalling MaxxAir N-Series Maxxfan rooftop ventilation fans because the printed circuit board may overheat, increasing the risk of a fire.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V397000·2026-06-19

    Indian Motorcycle Recalls 2026 Chief Vintage for Incorrect Rim Labeling

    Indian Motorcycle is recalling 2026 Chief Vintage models because the VIN label lists the wrong rear rim width, which could lead to improper tire mounting and loss of control.

    Product
    INDIAN — INDIAN CHIEF VINTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26563·2026-06-18

    Arrogantf Spa Drain Covers Recalled Over Entrapment and Drowning Hazards

    Arrogantf spa drain covers sold on Amazon violate federal safety standards and pose entrapment and drowning hazards. Consumers should stop using them immediately and contact the importer for a refund.

    Product
    Arrogantf Spa Drain Covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26562·2026-06-18

    GOPO Toys pull string teething toys reported to cause choking incidents

    About 70,410 GOPO Toys pull string teething toys are being recalled after three reports of the silicone strings reaching the back of a child's throat, causing respiratory distress or choking.

    Product
    GOPO TOYS Pull String Teething Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V394000·2026-06-18

    2026–2027 Cadillac Vistiq Third-Row Seat Power Fold Feature Recall

    General Motors is recalling 2026–2027 Cadillac Vistiq vehicles because the third-row power seatback may fail to reverse when it encounters a person, potentially trapping them.

    Product
    CADILLAC — CADILLAC VISTIQ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V395000·2026-06-18

    Farber Specialty Recalls 2025-2026 Emergency Vehicles Due to Touchscreen Failure

    Farber Specialty is recalling 2025-2026 HX620 and MCXCR emergency vehicles because the touchscreen may fail, preventing the activation of exterior lights and emergency equipment.

    Product
    FARBER SPECIALTY — FARBER SPECIALTY MCXCR, HX620 SBA 6X4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26568·2026-06-18

    Joolz Aer2 car seat adapters can detach, allowing the seat to fall

    About 3,840 Joolz Aer2 Car Seat Adapters are being recalled because they can fail to attach properly to the stroller, which may allow the car seat to fall.

    Product
    Joolz Aer2 Car Seat Adapters for Joolz Aer 2 Stroller
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26565·2026-06-18

    Arizer Solo III vaporizers recalled after four battery explosion reports

    About 5,000 Arizer Solo III Intergalactic (Black) portable vaporizers are being recalled after four reports of the internal lithium-ion battery exploding or igniting.

    Product
    Arizer Solo III portable electronic vaporizers (Intergalactic/Black color only)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26567·2026-06-18

    Children's Pajamas Recalled by SHEIN Over Burn Hazard

    SHEIN Distribution Corporation is recalling about 160 Michley children's pajamas that violate the mandatory flammability standard for children's sleepwear, posing a burn injury or death risk. No injuries have been reported.

    Product
    Michley Children's Pajamas
    Category
    Consumer Product
    Distribution
    Distributed nationwide